510(k) K221717
K221717 is an FDA 510(k) premarket notification submitted by Unimax Medical Products Co., Ltd. for the device "Disposable Surgical Gown UM-148". The FDA issued a decision of Substantially Equivalent on Sep 20, 2022. The device falls under product code FYA (Gown, Surgical), a Class II device regulated under 21 CFR 878.4040. Unimax Medical Products Co., Ltd. has 1 other 510(k) clearance on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Sep 20, 2022
- Date Received
- Jun 13, 2022
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Gown, Surgical
- Device Class
- Class II
- Regulation Number
- 878.4040
- Review Panel
- HO
- Submission Type
- 510(k)